SOX4型
脂肪变性
内分泌学
非酒精性脂肪肝
基因敲除
内科学
下调和上调
胰岛素抵抗
生物
转录因子
脂肪生成
睾丸决定因素
脂肪肝
甘油三酯
基因表达
基因
肥胖
医学
脂肪组织
发起人
胆固醇
疾病
遗传学
Y染色体
作者
Yang Jiao,J. Leon Zhao,Zhijian Zhang,Min Li,Yu Xi,Yanying Yang,Jie Liu,Shengjie Liao,Duanzhuo Li,Yuxing Wang,Die Zhang,Yulu Chen,Guojun Shi,Bin Liu,Yan Lu,Xiaoying Li
出处
期刊:Diabetes
[American Diabetes Association]
日期:2018-09-04
卷期号:67 (11): 2227-2238
被引量:22
摘要
Obesity is usually associated with an increased risk of nonalcoholic fatty liver disease that is characterized by accumulation of excessive triglyceride (TG) in hepatocytes. However, the factors involved in the obesity-induced hepatosteatosis are poorly defined. Here, we report that SRY-box containing gene 4 (Sox4), a transcription factor that regulates cell proliferation and differentiation, plays an important role in hepatic TG metabolism. Sox4 expression levels are markedly upregulated in livers of obese rodents and humans. Adenovirus-medicated overexpression of Sox4 in the livers of lean mice promotes liver steatosis, whereas liver-specific knockdown of Sox4 ameliorates TG accumulation and improves insulin resistance in obese mice. At the molecular level, we show that Sox4 could directly control the transcription of SREBP-1c gene through binding to its proximal promoter region. Thus, we have identified Sox4 as an important component of hepatic TG metabolism.
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